Canonical Allele Identifier: CA1729180867
Gene: CYP3A4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.99768383T= , CM000669.2:g.99768383T= GRCh38
NC_000007.13:g.99366006T= , CM000669.1:g.99366006T= GRCh37
NC_000007.12:g.99203942T= NCBI36
NG_008421.1:g.20803A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000336411.7:c.641A= ENSP00000337915.3:p.Asp214=
ENST00000651514.1:c.641A= MANE Select ENSP00000498939.1:p.Asp214=
ENST00000651783.1:c.182A= ENSP00000498924.1:p.Asp61=
ENST00000652018.1:c.494A= ENSP00000498733.1:p.Asp165=
ENST00000336411.6:c.641A= ENSP00000337915.2:p.Asp214=
ENST00000354593.6:c.191A= ENSP00000346607.2:p.Asp64=
NM_001202855.2:c.641A= NP_001189784.1:p.Asp214=
NM_017460.5:c.641A= NP_059488.2:p.Asp214=
XM_011515841.1:c.641A= XP_011514143.1:p.Asp214=
XM_011515842.1:c.641A= XP_011514144.1:p.Asp214=
NM_017460.6:c.641A= MANE Select NP_059488.2:p.Asp214=
NM_001202855.3:c.641A= NP_001189784.1:p.Asp214=